Variant report

Variant rs73291964
Chromosome Location chr12:46963079-46963080
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46956800-46963400 Weak transcription Aorta Aorta
2 chr12:46957000-46964800 Weak transcription NHDF-Ad bronchial
3 chr12:46960400-46963800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr12:46961600-46963600 ZNF genes & repeats Primary Natural Killer cells fromperipheralblood blood
5 chr12:46961600-46970800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:46962000-46963400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:46962800-46963200 ZNF genes & repeats Hela-S3 cervix
8 chr12:46962800-46963400 ZNF genes & repeats Gastric stomach
9 chr12:46962800-46964000 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
10 chr12:46962800-46964000 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
11 chr12:46962800-46964000 ZNF genes & repeats Fetal Intestine Small intestine
12 chr12:46963000-46963200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr12:46963000-46963400 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
14 chr12:46963000-46964000 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr12:46963000-46971200 Weak transcription Primary B cells from cord blood blood

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